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Ben Distel

Showing results (21-30 of 48) with videos related to

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Human Molecular Genetics|April 11, 2025
Localization of human UBE3A isoform 3 is highly sensitive to amino acid substitutions at p.Met21 positionAnnelot C M van Esbroeck, Rob F M Verhagen, Martina Biagioni, et al.
Eukaryotic Cell|December 31, 2014
Identification and characterization of Rvs162/Rvs167-3, a novel N-BAR heterodimer in the human fungal pathogen Candida albicansAreti Gkourtsa, Janny van den Burg, Karin Strijbis, et al.
International Journal of Molecular Sciences|January 8, 2023
The Hippocampal Response to Acute Corticosterone Elevation Is Altered in a Mouse Model for Angelman SyndromeEva M G Viho, A Mattijs Punt, Ben Distel, et al.
Microbiology (Reading, England)|October 4, 2008
The activity of the glyoxylate cycle in peroxisomes of Candida albicans depends on a functional beta-oxidation pathway: evidence for reduced metabolite transport across the peroxisomal membraneKatarzyna Piekarska, Guy Hardy, Els Mol, et al.
The Journal of Clinical Investigation|April 14, 2015
Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome modelSara Silva-Santos, Geeske M van Woerden, Caroline F Bruinsma, et al.
Eukaryotic Cell|September 12, 2006
Peroxisomal fatty acid beta-oxidation is not essential for virulence of Candida albicansKatarzyna Piekarska, Els Mol, Marlene van den Berg, et al.
The Journal of Biological Chemistry|June 5, 2010
Contributions of carnitine acetyltransferases to intracellular acetyl unit transport in Candida albicansKarin Strijbis, Carlo W van Roermund, Janny van den Burg, et al.
Human Molecular Genetics|September 4, 2020
Conserved UBE3A subcellular distribution between human and mice is facilitated by non-homologous isoformsF Isabella Zampeta, Monica Sonzogni, Eva Niggl, et al.
Human Molecular Genetics|February 19, 2021
Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutationsStijn N V Bossuyt, A Mattijs Punt, Ilona J de Graaf, et al.
Plos One|June 13, 2015
Evolution of the SH3 Domain Specificity Landscape in YeastsErik Verschueren, Matthias Spiess, Areti Gkourtsa, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|April 11, 2025
Localization of human UBE3A isoform 3 is highly sensitive to amino acid substitutions at p.Met21 positionAnnelot C M van Esbroeck, Rob F M Verhagen, Martina Biagioni, et al.
Eukaryotic Cell|December 31, 2014
Identification and characterization of Rvs162/Rvs167-3, a novel N-BAR heterodimer in the human fungal pathogen Candida albicansAreti Gkourtsa, Janny van den Burg, Karin Strijbis, et al.
International Journal of Molecular Sciences|January 8, 2023
The Hippocampal Response to Acute Corticosterone Elevation Is Altered in a Mouse Model for Angelman SyndromeEva M G Viho, A Mattijs Punt, Ben Distel, et al.
Microbiology (Reading, England)|October 4, 2008
The activity of the glyoxylate cycle in peroxisomes of Candida albicans depends on a functional beta-oxidation pathway: evidence for reduced metabolite transport across the peroxisomal membraneKatarzyna Piekarska, Guy Hardy, Els Mol, et al.
The Journal of Clinical Investigation|April 14, 2015
Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome modelSara Silva-Santos, Geeske M van Woerden, Caroline F Bruinsma, et al.
Eukaryotic Cell|September 12, 2006
Peroxisomal fatty acid beta-oxidation is not essential for virulence of Candida albicansKatarzyna Piekarska, Els Mol, Marlene van den Berg, et al.
The Journal of Biological Chemistry|June 5, 2010
Contributions of carnitine acetyltransferases to intracellular acetyl unit transport in Candida albicansKarin Strijbis, Carlo W van Roermund, Janny van den Burg, et al.
Human Molecular Genetics|September 4, 2020
Conserved UBE3A subcellular distribution between human and mice is facilitated by non-homologous isoformsF Isabella Zampeta, Monica Sonzogni, Eva Niggl, et al.
Human Molecular Genetics|February 19, 2021
Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutationsStijn N V Bossuyt, A Mattijs Punt, Ilona J de Graaf, et al.
Plos One|June 13, 2015
Evolution of the SH3 Domain Specificity Landscape in YeastsErik Verschueren, Matthias Spiess, Areti Gkourtsa, et al.
Pageof 5